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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 731608생성일: 2026년 10월 24일

2-Aminopyridine → HCID 24738180, 화합물

https://huagongshe.com/ko/reaction/731608

반응식

참여 물질

역할이름HCID투입량
반응물2-AminopyridineHCID 10439—
반응물Sodium BicarbonateHCID 516892—
반응물4-(Bromoacetyl)-5-methyl-3-phenylisoxazoleHCID 2735531—
용매EthanolHCID 702—
생성물HCID 24738180HCID 2473818055%

반응 단계

A mixture of 4-(bromoacetyl)-5-methyl-3-phenylisoxazole (commercially available) (140 mg, 0.5 mmol) and 2-aminopyridine (47 mg, 0.5 mmol) in ethanol (3.1 mL) was heated under reflux under argon for 3.5 h. Then another portion of 2-aminopyridine (24 mg, 0.25 mmol) was added and heating under reflux continued for another 1 h. The resulting mixture was then cooled to room temperature and then sodium hydrogen carbonate (63 mg, 0.75 mmol) added and the resulting mixture heated under reflux for 2 h. After cooling to room temperature, the mixture was poured onto water and extracted with ethyl acetate. The combined organic layers were then washed with water and brine, dried over sodium sulphate and evaporated to leave a yellow oil. Purification by chromatography (SiO2, heptane:ethyl acetate=100:0 to 50:50) afforded the title compound (76 mg, 55%) which was obtained as a light yellow gum. MS: m/e=276.0 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07585874B2
출처 데이터셋uspto-grants-2009_09
ORD IDord-696ff80f9aef4bb98014deb962024899
출처 메모uspto-grants-2009_09